Prolog Flashcards
Possible cancers in Lynch II aka hereditary nonpolyposis colorectal cancer
Endometrium
Ovary
Gastric tract
Small bowel
Mismatch repair genes affected in lynch II aka HNPCC
MLH1 MSH2 MSH6 PMS2 EPCAM
Lynch syndrome-associated endometrial cancer accounts for up to X% of all endometrial cancer
6%
germline TP53 mutations are associated with __ syndrome
Li–Fraumeni
Li-Fraumeni syndrome is associated with a high risk of what 5 kinds of cancer?
soft tissue sarcomas leukemia adrenocortical cancer breast cancer brain cancer
Overexpression of PTEN is associated with __
Cowden disease
Heritability of Cowden disease
autosomal dominant
Cowden disease is associated with what 3 cancers & what skin lesion?
breast cancer
thyroid cancer
endometrial cancer
benign mucocutaneous lesions
A 45-year-old woman is diagnosed with grade 2 endometrioid adenocarcinoma of the endometrium, and she undergoes hysterectomy, BSO, and LA. She has a family Hx that includes cancer of the breast, lung, and colon in first-degree relatives. The test that will best inform her of her risk of future cancer is immunohistochemical staining of tumor tissue for: (A) MLH1, MSH2 overexpression (B) BRCA1 mutation (C) progesterone receptor (D) TP53 mutation (E) PTEN mutation
(A) MLH1, MSH2 overexpression
lifetime risk of breast cancer for a woman who carries a BRCA1 or BRCA2 mutation
65–74%
lifetime risk of ovarian cancer for a woman with a BRCA1 mutation
39 – 46%
lifetime risk of ovarian cancer for a woman with a BRCA2 mutation
12 - 20%
Risk of what other malignancies in BRCA2?
prostate
pancreatic
melanoma
In BRCA, risk-reducing salpingo-oophorectomy decreases the risk of breast cancer by:
50%
In BRCA, Risk- reducing salpingo-oophorectomy decreases the risk of ovarian cancer by:
80 – 95%
For ovarian cancer in BRCA pts, Risk reduction after 5 years of use: X%
33% to 38%
A 42-year-old woman, G2P2, in whom breast cancer was diagnosed at age 38 years, comes to your office for her annual well-woman visit. Her family history is significant for a mother who was diagnosed with ovarian cancer at age 68 years and a maternal aunt who developed a low- malignant-potential tumor of the ovary in her 20s. Her risk of having an inherited predisposition for ovarian cancer or breast cancer is: (A) less than 1% (B) 1–10% (C) 11–20% (D) greater than 20%
(D) greater than 20%
A 45-year-old woman, para 2, has been hospitalized with symptoms of diplopia, vertigo, and dizziness for the past 10 days. Three days ago, she had a contrast MRI scan of the head, which was negative for mass effect, lesions, and plaques. She has an elevated platelet count of 800,000/mm3. A body CT is negative except for a 6-cm complex lesion in the left ovary. Mammography was negative 1 month ago. On physical exam, you confirm the neurologic deficits. Analysis of serum and CSF samples show elevated anti-Yo antibody levels. The best explanation for these findings is: (A) hemorrhagic stroke (B) embolic stroke (C) paraneoplastic syndrome (D) multiple sclerosis
(C) paraneoplastic syndrome
Anti-Y o progressive cerebellar degeneration most commonly is associated with:
ovarian or breast carcinoma
Elevated platelet count is often another paraneoplastic manifestation of ovarian cancer resulting from:
increased production of thrombopoietic cytokines in the tumor and host tissue
A 42 yo Asian woman w/ a history of molar pregnancy comes to your office 13 months after initial diagnosis. Her serum β-hCG level is 14,650 IU/L. You diagnose gestational trophoblastic neoplasia (GTN). Her exam shows a 1-cm vaginal lesion. Pelvic US shows a 4-cm intrauterine tumor. Chest, abdomen, and pelvic computed CT scans show a 2-cm lung lesion consistent with metastatic disease. Head MRI is negative for metastasis. Her age, β-hCG level, 4-cm intrauterine tumor, and total of 2 metastatic sites give her a modified WHO risk score of 5. The factor that increases her WHO score to 9 is:
(A) previous molar pregnancy
(B) interval from molar pregnancy to GTN diagnosis longer than 12 months
(C) vaginal metastasis on exam
(D) lung metastasis
(B) interval from molar pregnancy to GTN diagnosis
Treatment for GTN: stage I disease and low-risk (score less than 7) stage II and III disease
single-agent chemotherapy with either methotrexate or actinomycin D
Treatment for high-risk GTN disease: either stage IV disease or high-risk (score 7 or more) stage II and III disease,
multiagent chemo with or without site- directed surgery or radiotherapy
(1) Etoposide + methotrexate + actinomycin D + cyclophosphamide + vincristine (2) methotrexate + actinomycin D + cyclophosphamide
cyclophosphamide MOA
alkylating agent – prevents cell division by cross-linking DNA strands and decreasing DNA synthesis